Canonical Allele Identifier: PA236972
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 191547
ClinVar RCV Id: RCV000171769 RCV000306117 RCV000395598 RCV001082067 RCV001797657 RCV002354430 RCV003965229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777594.1:p.Val203Met
CA236970
NM_174934.4:c.607G>A